Canonical Allele Identifier: PA125499
Gene: HBB HGNC NCBI

Linked Data

ClinVar Variation Id: 15589
ClinVar RCV Id: RCV000016856
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000509.1:p.Ala129Pro
CA125498
NM_000518.5:c.385G>C